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Standard Industrial Clean Sterile Room Projects Professional One Stop Manufacturing Service
| Brand Name: | SHP |
| Model Number: | Customized |
| MOQ: | 50 square meters |
| Price: | $500.00/square meters 50-499 square meters |
| Payment Terms: | L/C,T/T |
| Supply Ability: | ≥1 set |
Standard sterile room
,Industrial sterile room
,One Stop Manufacturing sterile clean room
Standard Industrial Clean Sterile Room Projects Professional One Stop Manufacturing Service
Product Overview
Cleanroom Description
| Application | Pharmaceutical | Lab | Electronics |
| Cleanliness | Class 100–100000 or applicable ISO/GMP classification | ISO 5–8 or project-specific classification | ISO 5–8 or project-specific classification |
| Scope |
Structure part; Partition and ceiling panel; door and window,epoxy. |
HVAC part; AHU and chiller; Ducting and piping. |
Electrical part; Lamp,switch and socket; Distribution cabinet. |
| Service | Design and production | Construction and test | Validation and training |
| Wall/ceiling panel | Machine-made or Hand-made sandwich board |
| Clean room equipment | Air shower,FFU,Pass box,Laminar flow cabinet,hepa box |
| Cleanliness | Class 100-100000 |
| Purification system | HVAC, or AC conditioner+FFU |
| Floor | PVC anti-static floor or epoxy-based coating |
| Other addessores | stalinite window,LED panel light,Door,Hand wash sink,storage/shoe cabinet etc |
| Service | Design,manufacturing,construction |
Technical Specifications
| Item | Specification |
|---|---|
| Cleanroom Type | Modular Prefabricated Cleanroom |
| Cleanliness Level | Class 1000 |
| Structure | Modular Cleanroom Structure |
| Wall System | Cleanroom Panel System |
| HVAC System | Integrated HVAC System |
| Air Filtration | HEPA Filtration |
| Air Supply | FFU System |
| Temperature Control | Customized According to Project Requirements |
| Humidity Control | Customized According to Project Requirements |
| Pressure Control | Customized According to Project Requirements |
| Cleanroom Area | Customized According to Project Requirements |
| Application | Pharmaceutical, Biotechnology, Medical, Microelectronic and Other Controlled Manufacturing Environments |
| Installation | Prefabricated On-Site Assembly |
| Project Engineering | Cleanroom Structure, HVAC, Water Piping and Electrical System Design |
| Testing & Commissioning | Cleanroom Performance Testing and Data Recording |
| Expansion | Modular Configuration for Flexible Layout and Future Modification |
| Supporting Equipment | Pass Box, Air Shower, Clean Bench and Other Cleanroom Supporting Equipment |
| Customization | Layout, Dimensions, HVAC, Filtration and Supporting Equipment Can Be Customized |
Final specifications are determined according to the cleanroom classification, production process and project requirements.
Engineering Note:
Cleanroom performance parameters are determined during project design based on the required cleanliness classification, production process, room functions and applicable standards. Final operating values are confirmed in the project technical specification and verified during commissioning and testing where applicable.
Cleanroom Core Functions
1. Contaminate Control
2. Stable Production Environment
3. Support Product Quality
4. Support Equipment and Personnel Protection
5. Meet Industry Compliance
Cleanroom Applications
Pharmaceutical & Biotechnology
Modular cleanroom systems can be configured for pharmaceutical and biotechnology applications requiring controlled airborne contamination, environmental conditions and pressure relationships.
Laboratory & R&D
Prefabricated cleanrooms can be adapted for laboratory, testing and research environments according to the required cleanliness classification and process conditions.
Electronics & Semiconductor
Cleanroom configurations can support electronics and precision manufacturing processes where airborne particle and environmental control are important.
Medical & Healthcare
Cleanroom systems can be configured for selected medical, healthcare and controlled production environments according to applicable project requirements.
Integrated Cleanroom System Components
Complete Cleanroom Material and Equipment Supply
In addition to cleanroom engineering services, SHP supplies the partition-type cleanroom panels, built-in filtration frames, HVAC systems and cleanroom doors essential to turnkey cleanroom project delivery.
The following illustration presents the core systems and products supplied within SHP cleanroom projects.
Engineering Workflow
Cleanroom Project Delivery Process
1. Requirement Assessment
Review cleanliness classification, production process and site requirements.
2. Engineering Design
Develop the cleanroom layout, enclosure, HVAC, filtration and related systems.
3. Manufacturing & Preparation
Manufacture or prepare cleanroom panels, equipment and supporting components.
4. Installation
Complete cleanroom enclosure, HVAC, electrical and related system installation.
5. Testing & Commissioning
Conduct agreed cleanroom performance tests and system commissioning.
6. Validation & Handover
Complete applicable validation, documentation and project acceptance.
Mauritius Project
Pharmaceutical Cleanroom Project – Mauritius
Project Overview
In Mauritius, SHP completed a turnkey pharmaceutical cleanroom project including design, manufacturing, HVAC installation, commissioning and final validation.
Project Information
| Item | Details |
| Location | Mauritius |
| Industry | Pharmaceutical Manufacturing |
| Solution | Turnkey Cleanroom Project |
| Scope | Design, HVAC, Installation, Validation |
| Cleanroom Class | ISO 7 |
| Status | Successfully Delivered |
Project Challenges
The project required a GMP-compliant production environment with strict control of airborne particles, temperature, humidity and differential pressure to support pharmaceutical production.
SHP Solution
- Modular cleanroom panel system
- Air handling unit (AHU) system
- HEPA filtration system
- Environmental monitoring system
- Pressure control system
Cleanroom Construction Progress Record
Cleanroom Panel Delivery and Material Preparation
Cleanroom wall and ceiling panels were delivered to the project site and organized according to the installation schedule. All materials were inspected before installation to ensure compliance with project specifications and cleanroom construction requirements.
HVAC Ductwork Fabrication and Installation
The HVAC installation team carried out on-site ductwork fabrication and assembly for the cleanroom ventilation system. Proper duct routing and sealing are essential for maintaining airflow uniformity, pressure control and contamination prevention.
Cleanroom Ceiling Grid and Utility Framework Installation
The ceiling suspension system and utility support framework were installed to accommodate cleanroom panels, lighting fixtures, HEPA filtration units and process utilities. This stage forms the structural foundation for the final cleanroom enclosure.
Project Completion
Cleanroom system installation completed
HVAC installation and commissioning completed
Cleanroom performance testing conducted
Project validation and acceptance completed according to the agreed project requirements
AVB Testing Report
Third-Party Performance Testing & Validation
Independent testing and validation were conducted after project completion to verify cleanroom performance and environmental control effectiveness.
Validation Services
- Design Qualification (DQ)
- Installation Qualification (IQ)
- Operational Qualification (OQ)
- Performance Qualification (PQ)
Testing Items
- Airborne Particle Count Test
- Airflow Velocity Test
- Differential Pressure Test
- Temperature Test
- Humidity Test
- Illumination Test
- Noise Test
Third-Party Verification
The cleanroom system was tested and documented by an independent testing organization to verify compliance with project specifications and applicable cleanroom standards.
Testing Evidence
The available test documentation records cleanroom performance measurements conducted after system installation and commissioning.
Project Evidence and Verification
The project information and construction photographs below are presented as documented project experience. Testing and performance information is provided where supported by the available project documentation and third-party test records.
